• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards | Inspections
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameTENNANT(TM) & KELMAN(TM) TYPE II
Classification Nametransducer, ultrasonic, obstetric
Generic Nameintraocular lens, anterior chamber
Regulation Number884.2960
ApplicantPRECISION-COSMET CO., INC.
PMA NumberP800016
Supplement NumberS001
Date Received03/23/1983
Decision Date05/25/1983
Product Code
HGL[ Registered Establishments with HGL ]
Advisory Committee Neurology
Expedited Review Granted? No
Combination Product No
-
-